| Literature DB >> 28537400 |
Ya-Long Zhang1, Xu-Wei Zhou1, Xiao-Bing Wang1, Lin Wu1, Ming-Hua Yang1, Jun Luo1, Yong Yin1, Jian-Guang Luo1, Ling-Yi Kong1.
Abstract
Xylopiana A (1), a dimeric guaiane with an unprecedented pentacyclo[5.2.1.01,2.04,5'.05,4']decane-3,2'-dione core, and three biosynthetically related intermediates, compounds 2-4, were isolated from the leaves of Xylopia vielana. Their structures and absolute configurations were determined by a combination of spectroscopic data, X-ray crystallography, electronic circular dichroism calculations, and chemical conversion. The structure of known vielanin A was revised to be compound 3. Compound 4 exerted a 3.7-fold potentiation effect on doxorubicin susceptibility at the tested concentration of 10 μM.Entities:
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Year: 2017 PMID: 28537400 DOI: 10.1021/acs.orglett.7b01276
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005